A high yield and rapid synthesis of enantiomerically pure N (alpha) -protected amino/peptide acid arylamides using n-propylphosphonic anhydride (T3P) in presence of N-methylmorpholine is described. The generality of the reaction has been studied for various N (alpha) -protected amino acids with diverse range of aromatic amines and coumarin derivatives
β-Amino acids X-NHCHRCH2CO2H (X = Z, Boc, or Fmoc protecting group; R = PhCH2, Me2CH, Ph, Me) were...
Abstract: The direct conversion of simple and sterically hindered Nα-protected amino/peptide hydrox...
Herein we demonstrate a chemoselective reaction of Nβ-protected amino alkyl sulfonyl azides with in ...
A high yield and rapid synthesis of enantiomerically pure N α -protected amino/peptide acid arylamid...
Thioacids derived from N-protected amino or dipeptide and tripeptide acids undergo facile N-acylatio...
A general, mild, efficient, and environmentally benign protocol, which makes use of T3P® as an acid ...
One-pot preparation of N α -protected amino/peptide hydroxamic acids from corresponding carboxylic a...
Synthesis of short peptides using propargyloxycarbonyl amino acid chlorides as effective coupling re...
Synthesis of short peptides using propargyloxycarbonyl amino acid chlorides as effective coupling re...
A mild and cost-efficient chemo-enzymatic method for the synthesis of C-terminal arylamides of amino...
A mild and cost-efficient chemo-enzymatic method for the synthesis of C-terminal arylamides of amino...
A simple and efficient method for the synthesis of alcohols from the corresponding carboxylic acids ...
The direct conversion of simple and sterically hindered Nα-protected amino/peptide hydroxamic acids ...
Peptide bond forming reactions are fundamental to the synthesis of peptides and peptidomimetics. Unf...
Peptide bond forming reactions are fundamental to the synthesis of peptides and peptidomimetics. Unf...
β-Amino acids X-NHCHRCH2CO2H (X = Z, Boc, or Fmoc protecting group; R = PhCH2, Me2CH, Ph, Me) were...
Abstract: The direct conversion of simple and sterically hindered Nα-protected amino/peptide hydrox...
Herein we demonstrate a chemoselective reaction of Nβ-protected amino alkyl sulfonyl azides with in ...
A high yield and rapid synthesis of enantiomerically pure N α -protected amino/peptide acid arylamid...
Thioacids derived from N-protected amino or dipeptide and tripeptide acids undergo facile N-acylatio...
A general, mild, efficient, and environmentally benign protocol, which makes use of T3P® as an acid ...
One-pot preparation of N α -protected amino/peptide hydroxamic acids from corresponding carboxylic a...
Synthesis of short peptides using propargyloxycarbonyl amino acid chlorides as effective coupling re...
Synthesis of short peptides using propargyloxycarbonyl amino acid chlorides as effective coupling re...
A mild and cost-efficient chemo-enzymatic method for the synthesis of C-terminal arylamides of amino...
A mild and cost-efficient chemo-enzymatic method for the synthesis of C-terminal arylamides of amino...
A simple and efficient method for the synthesis of alcohols from the corresponding carboxylic acids ...
The direct conversion of simple and sterically hindered Nα-protected amino/peptide hydroxamic acids ...
Peptide bond forming reactions are fundamental to the synthesis of peptides and peptidomimetics. Unf...
Peptide bond forming reactions are fundamental to the synthesis of peptides and peptidomimetics. Unf...
β-Amino acids X-NHCHRCH2CO2H (X = Z, Boc, or Fmoc protecting group; R = PhCH2, Me2CH, Ph, Me) were...
Abstract: The direct conversion of simple and sterically hindered Nα-protected amino/peptide hydrox...
Herein we demonstrate a chemoselective reaction of Nβ-protected amino alkyl sulfonyl azides with in ...